A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3697n223



Internal ID22806665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:52495165..52544718hg38UCSC Ensembl
chr19:52998418..53047971hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3849554
hg1949554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6519058, nsv6517390
Samples
Known GenesZNF578, ZNF808
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3697n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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